{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lewis Center",
      "address_1": "741 Radio Dr",
      "reason_for_recall": "Labeling: Label Mix up; product labeled to contain Docusate Sodium 240mg instead of Docusate Calcium 240mg",
      "address_2": "",
      "product_quantity": "99/240 mg softgel caps",
      "code_info": "Lot #: 002H79, Use By: 06/19/2013, NDC: 00904-5779-60",
      "center_classification_date": "20140723",
      "distribution_pattern": "Product was shipped to the following states: CO, MA, OH, TX & WY.",
      "state": "OH",
      "product_description": "Docusate Calcium Softgel Capsules, 240 mg, OTC, packaged and labeled to contain Docusate Sodium 240mg, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Major Pharmaceuticals, Livonia, MI  NDC 00904-5779-60",
      "report_date": "20140730",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Shamrock Medical Solutions Group LLC",
      "recall_number": "D-1451-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "64611",
      "termination_date": "20140731",
      "more_code_info": "",
      "recall_initiation_date": "20110927",
      "postal_code": "43035-7134",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}